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ABX Pentra ASO 2 CP - Indonesia BPOM Medical Device Registration

ABX Pentra ASO 2 CP is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303810671. The device is manufactured by DENKA SEIKEN CO. LTD,. KAGAMIDA FACTORY. from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is HORIBA INDONESIA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : C
ABX Pentra ASO 2 CP
Analysis ID: AKL 20303810671

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

HORIBA INDONESIA

AR Address

Jl. Jalur Sutera , Blok. 20A, No. 16 - 17, Kel. Kunciran, Kec. Pinang

Registration Date

Mar 10, 2023

Expiry Date

Dec 31, 2028

Product Type

Serological Reagents

Streptococcus spp. serological reagents.

Invitro Diagnostics

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